Gene Details



LIPH and homologs in 1 species are found in 85 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 2112 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier III Human 2616 Genes GS218390: Alcoholism Susceptibility Chr 1
Expand Tier I Human 22 Genes GS174676: HP:0002217 Slow-growing hair
Expand Tier I Human GO 252 Genes GS194309: GO:0016042 lipid catabolic process
Expand Tier I Human 48 Genes GS174713: HP:0002213 Fine hair
Expand Tier I Human GO 112 Genes GS199036: GO:0016298 lipase activity
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Human GO 95 Genes GS210231: GO:0004620 phospholipase activity
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 24 Genes GS172624: HP:0000653 Sparse eyelashes
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 113 Genes GS176227: HP:0010719 Abnormality of hair texture
Expand Tier I Human 174 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier I Human GO 131 Genes GS207420: GO:0008201 heparin binding
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human CTD 1151 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Human GO 173 Genes GS209592: GO:0005539 glycosaminoglycan binding
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human GO 731 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 9 Genes GS173361: HP:0004540 Congenital, generalized hypertrichosis
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 54 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 153 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 22 Genes GS171659: HP:0000615 Abnormality of the pupil
Expand Tier I Human 88 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 1137 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human GO 851 Genes GS203972: GO:0005615 extracellular space
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 22 Genes GS171992: HP:0011363 Abnormality of hair growth rate
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 50 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Human 15 Genes GS176920: HP:0002224 Woolly hair
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human 49 Genes GS175085: HP:0000989 Pruritus
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 1094 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human GO 1994 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human 69 Genes GS171136: HP:0100840 Aplasia/Hypoplasia of the eyebrow
Expand Tier I Human GO 188 Genes GS201611: GO:0097367 carbohydrate derivative binding
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 93 Genes GS174190: HP:0001596 Alopecia
Expand Tier I Human 194 Genes GS173872: HP:0011368 Epidermal thickening